FDA inspection

Hiossen Inc.: FDA inspection ending Apr 12, 2017

FDA inspection 1007913 · Voluntary Action Indicated (VAI) · Fairless Hills, PA

Key facts

Inspection ID 1007913
Firm Hiossen Inc.
FEI number 3007135442
Address Keystone Industrial Port Complex, 85 Ben Fairless Dr
City Fairless Hills
State PA
ZIP 19030
Country United States
Fiscal year 2017
Inspection end date Apr 12, 2017
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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